Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300921 | |||||||||||||||||||||||||||||||||||||||||
Literature Links: |
BHLHB9 PubMed Links | |||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
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Global
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Caucasian - Not Available | CEPH (CEU)
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EAS
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African American - Not Available | YRI (Yoruba) - Not Available | ||||||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | ||||||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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BHLHB9 - basic helix-loop-helix domain containing, class B, 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001142524.1 | 1029 | Missense Mutation | AGT,GGT | S,G 132 | NP_001135996.1 | |
NM_001142525.1 | 1029 | Missense Mutation | AGT,GGT | S,G 132 | NP_001135997.1 | |
NM_001142526.1 | 1029 | Intron | NP_001135998.1 | |||
NM_001142527.1 | 1029 | Intron | NP_001135999.1 | |||
NM_001142528.1 | 1029 | Intron | NP_001136000.1 | |||
NM_001142529.1 | 1029 | Intron | NP_001136001.1 | |||
NM_001142530.1 | 1029 | Intron | NP_001136002.1 | |||
NM_030639.2 | 1029 | Missense Mutation | AGT,GGT | S,G 132 | NP_085142.1 |
Set Membership: |
HapMap |